Pediatric Endocrine and Cardiovascular Study Notes, Study Guides, Projects, Research of Pediatrics

Study notes on pediatric endocrine and cardiovascular conditions. It covers precocious puberty, growth hormone deficiency, glucose levels, and insulin types. Cardiovascular topics include congenital heart defects (chd) such as patent ductus arteriosus (pda), atrial septal defect (asd), ventricular septal defect (vsd), and coarctation of the aorta (coa), as well as cyanotic defects like tetralogy of fallot (tof) and hypoplastic left heart syndrome (hlhs). The notes detail symptoms, treatments, and nursing considerations for managing these conditions in pediatric patients, including medication administration and monitoring for complications. It also includes information about pediatric assessment scales like gcs and pews.

Typology: Study Guides, Projects, Research

2024/2025

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Ped Exam 3 Study Notes
ENDOCRINE:
Precocious Puberty (too early):
Puberty begins before age 8 in girls and before age 9 in boys
Height and weight curve would be earlier than normal
Early closure of growth plate resulting in less than normal height for age
Labs:
Elevated GH - which includes LH and FSH
Assessment:
Labs
Growth percentiles
Tanner stage
Bone age
IDIOPATHIC in girls; PATHOLOGIC in boys
Treatment:
Stop and reverse onset of puberty
Types:
Central = most common (90-95%)
Onset of puberty in usual pattern
Pituitary switch turns on too early
Treatment = meds to stop process until age we want it to occur
LUPRON:
Injections q3 months or 1 month
Most puberty signs will reverse
On medication until we think puberty would
start
Missing dose = symptoms will come back
Peripheral =
Some elements of puberty occur but not all- showing out of
order as well
Estrogen and testosterone levels are increasing
Usually related to problem like tumor
Incomplete =
No progression of puberty
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Ped Exam 3 Study Notes

ENDOCRINE:

● Precocious Puberty (too early): ○ Puberty begins before age 8 in girls and before age 9 in boys ○ Height and weight curve would be earlier than normal ○ Early closure of growth plate resulting in less than normal height for age ○ Labs: ■ Elevated GH - which includes LH and FSH ○ Assessment: ■ Labs ■ Growth percentiles ■ Tanner stage ■ Bone age ○ IDIOPATHIC in girls; PATHOLOGIC in boys ○ Treatment: ■ Stop and reverse onset of puberty ○ Types: ■ Central = most common (90-95%) ● Onset of puberty in usual pattern ● Pituitary switch turns on too early ● Treatment = meds to stop process until age we want it to occur ○ LUPRON: ■ Injections q3 months or 1 month ■ Most puberty signs will reverse ■ On medication until we think puberty would start ■ Missing dose = symptoms will come back ■ Peripheral = ● Some elements of puberty occur but not all- showing out of order as well ● Estrogen and testosterone levels are increasing ● Usually related to problem like tumor ■ Incomplete = ● No progression of puberty

● See something happen and then it reverses itself ○ Ex: one boob grows, other doesn’t, then it retreats ○ Gynecomastia ● Possibly from a random surge of hormones- then quiets down ● Growth Hormone Deficiency (GHD): ○ Weight percentile exceeds height (weight is following normal curve - height falls off grid) ○ Immature facial appearance (baby face) ○ Frontal bossing - frontal bone protrudes out ○ Can affect voice (high pitched), genitals ○ Trunk = looks obese cause height is lacking ○ Labs = low GH ● GCS: ○ Pediatric scale used for children under 5 ○ Normal range is 13- 15 ○ ABNORMAL = UNDER 8, INTUBATE ● PEWS: pediatric early warning score ○ Score above 7 = RRT ○ 4-6 = notifying something ○ 03 = no action ● GLUCOSE LEVELS: ● INSULIN: Type Trade Name Onset Peak Duration

Intermediate NPH insulin (Humulin N; Novolin N) 2-6 hrs. 4-14 hrs. 14-20 hrs. Long acting Insulin Glargine (Lantus) Detemir (Levemir) 1 hr. None or small peak after 10-16 hrs. 20-24 hrs. CARDIOVASCULAR: ● Clues that something is wrong = FEAR ○ F = feeding poorly; uses so much energy, breathing too fast ○ E = energy low; always tired, head bobbing, always napping ○ A = always fussy; grunting, crying ○ R = rapid respirations; low oxygen sat ● Congenital Heart Defect Symptoms: ○ Increased pulse ○ Increased respirations ○ FTT ○ Dyspnea, Orthopnea ○ Fatigue ○ URI ● *MOST FREQUENT SIGN OF CHD: ○ Increased RR first ○ Edema also seen in most dependent part ■ For babies = sacrum, bottom ■ Once walking = legs ● Most frequent complaint from parents of infants with CHD: ○ Child isn’t eating enough, losing weight ○ Insensible loss = breathing so fast that they lose weight ● Little helpful hint = ○ Defect begins with T : Cyanotic ■ blue ○ Defects begin with A : Acyanotic ■ Pink

“Acyanotic” Defects:

● General information: ○ Blood shunts from Left to Right

○ Leading to Increased pulmonary blood flow ○ Absence of cyanosis- skin remains pink ○ Symptoms: ■ Pt is typically asymptomatic ■ Murmur is present with or without symptoms ■ s/s of CHF could be present ■ Can experience fatigue related to increased pulmonary blood flow ○ Treatments: ■ Wait and see… hole can close on own ■ Meds: ● Digoxin and Furosemide ○ Given for heart failure! ○ Working = symptoms are going away ■ Surgery ● Patch to close hole- simple surgery ● Discussed if hole hasn’t closed on its own by 2y.o. ● Usually fixed between 2-5y.o. ● Types: ○ Patent Ductus Arteriosus (PDA): ■ Cause = Ductus Arteriosus doesn’t close at birth ● Ductus Arteriosus = tunnel connecting aorta and pulmonary artery ■ Symptoms = ● Skin remains pink ● s/s of HF ● Can be asymptomatic ■ Treatment = ● Symptomatic at birth - 28d (neonate) ○ Indomethacin or ibuprofen ■ Must be given in NICU setting ■ Medically closes the heart ■ ONLY GIVEN TO NEONATE ● Past 28d (not neonate) ○ Digoxin and Furosemide ● If no response to medication = surgery ○ Atrial Septal Defect (ASD): ■ Cause = foramen ovale fails to close at birth ● Foramen ovale = hole between atria ■ Symptoms = ● Skin remains pink

○ Exhibits signs of HF ○ Treatment: ■ Prostaglandin E

● Not at birth: ● Temporary fix ● Keeps ductus arteriosus open until surgery is possible ○ Found from hearing a murmur or seen on echo ○ Treatment: ■ Surgical fix ● Teen years: ○ Found when symptoms appear upon exercise ○ Trouble breathing, leg cramps, headache ■ Treatment = ● Surgical removal of stenosed area ● Surgical widening of aorta - slice vessel open, puts patch over opening to make vessel larger ● Balloon angioplasty with stent ● Treatment of hypertension = ACE inhibitor

“Cyanotic Defects”

● General information: ○ Blood shunts from Right to Left ○ Leading to decreased pulmonary blood flow ○ Symptoms = ■ Severe Cyanosis ■ Hypoxemia ● Hypoxemia is expected. Baseline O2 might be in 80s ■ Polycythemia ■ Clubbing ■ Hypercyanotic Tet spells ○ Requires surgery and medication ● Tet spell = hyper-cyanotic spell ○ Cause = stimuli, bearing down, crying, anger ○ Baseline cyanosis worsens to bluer than normal ○ Treatment = ■ MUST REVERSE! ■ First = put in position that increases pulmonary blood flow ● Knee-chest position ○ Pushed blood from lower parts of body to pulmonary system ● This can be accomplished by placing them in this position or asking them to squat

● Blood shunts from L to R → increased pulmonary blood flow ■ Stenosis of entrance to pulmonary artery and valve ● Causes blood to be stuck in R side → hypertrophy ■ Right Ventricular Hypertrophy ● Occurs from stenosis of pulmonary artery and valve ■ Overarching Aorta: ● Aorta connects to VSD ● Unoxygenated blood from RV travels into Aorta and into systemic circulation ○ Symptoms = ■ Range r/t severity of shunting of blood into aorta and size of holes ■ Symptomatic at birth: ● Baby presents with cyanosis and distress ■ Known before birth: ● Baby given HF medication ● Scheduled for surgery later on ○ Treatment = ■ Symptomatic at birth: ● Given Prostaglandin E to keep Ductus Arteriosus open in order to send to surgery ● Intubation, NPO, IV fluids, frequent vitals ● Surgery = temporary shunt to allow blood to flow/shift and not congregate ■ Doing well on HF meds: ● Continue meds ● Schedule surgery later on ○ Surgery = stenosis is the big thing that needs to be fixed! ■ Patch to enlarge stenosed pathway from RV to PA ■ Patch to close opening between ventricles ● Hypoplastic Left Heart Syndrome (HLHS) ○ Cause = born with the left side of heart underdeveloped ○ Symptoms = ????? can’t function - would know beforehand ○ Treatment = ■ *** Prostaglandin E ● Need to keep heart open so they can live until immediate surgery is performed ■ SURGERY ● 3 part process ● First surgery is done immediately after birth ■ Parent can decide if they want to let child peacefully die ■ Heart Transplant is best-case scenario

■ HF medications ■ Anticoagulants throughout surgeries ○ SURGERY:

● Potassium Levels: ○ Hyperkalemia can enhance effects of digoxin → toxicity ○ Important to check ● S/S of toxicity:

○ Nausea (reminder that not all children can say this) ○ Vomiting ○ Diarrhea ○ Lethargy ○ Bradycardia HYPOTENSION: ●

Definition of Hypotension by Systolic Blood Pressure and Age

Age Systolic Blood Pressure

Neonates < 60 mm Hg

Infants (1 to 12 months) <70 mm Hg

Children 1 to 10 years (5th BP

percentile)

<70 mm Hg + (age in years x 2) mm Hg

Children > 10 years <90 mm Hg

● Hypotension is a LATE indicator of cardiac decompensation CARDIAC ASSESSMENT REMINDERS: ● APETM ● Apical HR listened to at 4th ICS < 7y.o ● Apical HR listened to at 5th ICS > 7y.o. ● Indicators of Cardiac Dysfunction: ○ Poor feeding ○ tachypnea/tachycardia ○ FTT/poor weight gain/activity intolerance ○ Developmental delays ○ Thrills, Heaves ○ Prenatal history: ■ Rubella ■ Alcoholism ■ DM ■ Lupus ■ Advanced maternal age ■ Teratogenic meds ○ Dysrhythmias: ■ Bradycardia ■ Tachycardia

■ Normal sinus arrhythmia ● 5 Lead Placement: ○ RL = right leg (placed on R lower abdomen) ○ LL = left leg (placed on L lower abdomen) ○ RA = right arm (placed under the R clavicle MCL) ○ LA = left arm (placed under the L clavicle MCL) ○ V1 = ventricular lead (placed at 4th ICS right sternal border) ● 3 Lead Placement: ○ RA = right arm (placed under R clavicle MCL) ○ LA = left arm (placed under L clavicle MCL) ○ LL = left leg (placed on the left lower abdomen)

HYPOKALEMIA:

● Foods to give that are high in potassium ○ Potatoes, Pork ○ Oranges ○ Tomatoes ○ Avocados ○ Strawberries ○ Spinach ○ Fish ○ Mushrooms ○ Musk melons - cantaloupe INFECTIOUS AND INFLAMMATORY CARDIAC DISORDERS ● Rheumatic Fever: ○ Inflammatory heart condition occurring post pharyngitis (strep) ■ Strep can spread → valve damage ○ JONES CRITERIA: need 2 major OR 1 major and 2 minor for diagnosisNeed positive throat culture or ASO titer ■ Major Criteria: ● Chorea ○ Tick/involuntary movements ○ Sticks around for long time ● Carditis ○ Inflammation of the heart muscle ○ Can lead to valve damage (aortic and mitral valves) ○ Assessment: ■ Murmur or friction rub ■ Echocardiogram

■ Chest pain, may see signs of HF ○ Seen early on; short lived ● Erythema Marginatum

● Sores, cracked lips, bleeding ● Strawberry tongue ○ Treatment = ■ Phases

● Acute phase = high fever for 5+ days ● Sub-acute phase = fever subsides and onset of other symptoms arise ● Convalescence = abnormal labs linger (elevated SED rate, C-reactive protein/CRP) thrombocytosis (high level of platelets) ■ MEDS ● IVIG: one dose ○ Given and checked like a blood product; many vitals and assessing ○ Given over 8-12 hrs ○ Usually subsides the fever right away ● High dose Aspirin = 80-100mg/kg/day ○ Given until fever goes away ● Low dose Aspirin = 3-5 mg/kg/day ○ Given when fever is gone ○ For antiplatelet use ● * no ibuprofen ■ COMFORT: ● Ice pops, magic mouthwash for mouth ● Lotion for skin ● Chapstick or something for lips ● Cluster care ■ Telemetry!!! ■ Echocardiogram ■ Notes = ● aspirin is ototoxic ● Pt cannot receive other meds with aspirin in it ● Multisystem Inflammatory Syndrome-COVID (MIS-C) ○ Patients must be <21y.o. ○ Symptoms = ■ Must present with: ● Fever ● Elevated ESR & CRP ● Shows >= 2 organ involvement ● +covid now, exposure, or +covid within 4 weeks ■ Labs: ● Elevated troponin ● BNP elevation ● Elevated CRP ● Elevated ESR ○ Treatment =